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Good News For Commercial Reprocessors In Commission’s Draft Implementing Act On SUDs

 
• By Amanda Maxwell

Reprocessing is not going to be easy for hospitals in-house, putting the likely market into the hands of commercial reprocessors. What do we know about how the outlook is shaping up from the draft Commission Implementing Regulation, an implementing act now moving well down the pipeline?

Lab_Cleaning

Most EU hospitals are not equipped to comply with level of stringency demanded in the draft European Commission Implementing Regulation that lays down rules for the application of the EU Medical Devices Regulation as regards common specifications for the reprocessing of single-use devices. 

That is the view of Dan Vukelich, president of the Association of Medical Device Reprocessors

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More from Europe

Inclusive By Design: UK Invites Sponsors To Submit Trial Diversity Plans

 
• By Vibha Sharma

The UK has issued clearer guidance to help drug and medical device sponsors demonstrate how they intend to include a diverse and relevant range of participants in their clinical trials.

Plans For Specific EU Orphan And Pediatric Device Expert Panel Need To Go Further

 
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More from Geography

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Disparities — Including Financials Shortcomings — Remain In Women’s Health, Execs Say

 
• By Brian Bossetta

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